HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224431Generated: October 30, 2026
Hydrochloric Acid → HCID 12878340, compound
https://huagongshe.com/reaction/224431
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1-Cyclohexyl-3-methoxybenzene | HCID 12878339 | — |
| Solvent | 1,1,1,2-Tetrachloroethane | HCID 12418 | — |
| Product | HCID 12878340 | HCID 12878340 | — |
Reaction Steps
70 g of AlCl3 are added with stirring at -5° to 47.5 g of m-cyclohexylanisole, 26.5 g of succinic acid anhydride, 250 ml of tetrachloroethane and 62.5 ml of nitrobenzene, at such a rate that the temperature does not exceed -5°. The mixture is then stirred for 72 hours at 22°. 2N hydrochloric acid is then slowly added in the cold to the reaction solution until there is no further reaction, and the solution is then extracted twice with methylene chloride. The organic phases are extracted with 2N NaOH. The alkaline extract is acidified and extracted there times with ethyl acetate. The ethyl acetate phases are washed three times with water, dried over Na2SO4 and evaporated. The residue is crystallised twice from methylene chloridehexane. M.p. 130°-131°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04232039 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-5ea0c129e25641708c683d4ff8c8227a |
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| Source note | uspto-grants-1980_11 |
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